| Tag | Content |
|---|
EnhancerAtlas ID | HS098-14787 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:122203170-122204990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:122203598-122203616 | GGGAGGGAGCAAGGCAGG | + | 6.33 | | FOS | MA0476.1 | chr12:122203642-122203653 | TGTGACTCATC | + | 6.14 | | JUND | MA0491.1 | chr12:122203642-122203653 | TGTGACTCATC | + | 6.14 | | NFYA | MA0060.3 | chr12:122204468-122204479 | TCTGATTGGCC | - | 6.02 | | NFYB | MA0502.1 | chr12:122204542-122204557 | CTGATTGGTTGGCTG | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr12:122203254-122203269 | TGAACTCCTGACCTC | - | 6.22 | | RELA | MA0107.1 | chr12:122204290-122204300 | GGGAATTTCC | + | 6.02 | | ZNF263 | MA0528.1 | chr12:122203682-122203703 | CCCTCCTCCAGCTCCTCCTCA | - | 7.05 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 122203939 | 122204231 | | chr12 | 122203453 | 122203904 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I121765 | chr12 | 122203081 | 122206677 |
|
Enhancer Sequence | GATTAGAGGT GCACACCACC ATGCCTAGCT AATTTTTGTA TTTTTAGTAG AGATGGGGTT 60
TCACCGTGCT GGCCAGGCTG ATCTTGAACT CCTGACCTCA GGTGATCTGC TCACCTCGGC 120
CTTCTGAAGT GCTGGGATTA GAGGCATGAG CCACTGTGCC CAGCCCCGAG TTTTTTTTAC 180
TAAGGACCTT TTATGGCATA TATGGTTCAA GGAATTTGAG GTTGCAATGG AACCATTCCT 240
CCAGGCCTGT CTCCCCTTGG TGGTCTGAGG CAGGGGTTTG AATGGGCAAG TGGAGTCTGG 300
AATGGGGCCT CTGGGCCCAA ATAGATGCAT TATCTTCTAT TTAGGTTAGT CTAAAAGTAT 360
TTGTGTTTTG CAGTCATTTT TTGCACCAAC CTAATAGAAG GACTACAGGA GCTGGGGCCA 420
GCTTGTCGGG GAGGGAGCAA GGCAGGTGGG CTAAATCCGA GTGACTCATA CTTGTGACTC 480
ATCTTCCACA TCTGTTGGAG ATTTAGCCTC CGCCCTCCTC CAGCTCCTCC TCAGGGCTGA 540
TTGATCCTGG GGGCAGGCAA GGGAGATGCC TTGGAGGCCT CCCCTCCTGC TTGGTTCTTT 600
ACCAGGGAGT AGCTCAGAAG CCCTTGCAGG AGAGCCTGTG TGGAGGCGGT GGGAGGTGAG 660
ACTGGGATGA ACTCTAGTTT CTCATCCCTG AAGCATCCAC TCACTCGGGG CTGGTGCGCG 720
CCGTCAACAC CCCACAGTCT TTGCCGAAGT GACCCAAACC CAAGTTCTGC GTGAGGAAGG 780
GTCCTGGGGC CATCACGGCA TTCTAGAGAC GGCGTCGCTG AACCCTACGG GCCTCCTGGG 840
GGCCTGCTGC CCTGTTTTGT CTGATGGAGG CGCTTTTGTC CAGTTCTGGC TGCACCTGAG 900
ATTTGAATTG GGACAGGAGG TGTGGTCAGG GGAGCAGGTA GGGGTGGGGA CTTCCTCATC 960
GAGATATGAA GCCACCCTCG GTTTGTGTCT GGTGCCTGCC AAGTGAGATG CCACTCATCA 1020
GCTCAGCATA ATAAGCAAGT CAGCTCTTGT AAACTTGAAA ATGATGGAAA ACCATCCCAT 1080
AGGGACTAAA CCTGAAGGGG TCTTATGGGC CCATGTAACT GGGAATTTCC ATTCAAGGAG 1140
GTCAGGAGGG CTCAGGAGGT GTTCATGGCC CGGCTCCAGC TCCCTGTTCT GTTTTCCCCT 1200
GCGATGGCCC CCAGCGGCCC CCAGGCAGGC CTCCCACCAG CAGTAACCCC TGGGCTGACA 1260
GACCTCCCTC CACCCCAGTT GGAATCTTGA CACAGACTTC TGATTGGCCA GGCTTGGGTG 1320
ACCTACTGAT CTCTGAGAGC CAGTCACTGT TGCCAGAGGA CTGCAGAGGG TCCTGATTGG 1380
TTGGCTGGGG GTCATGTGCT TGGGTATAAG ACTGTGGTCT ATCCCAGCCA CCCAGACTGA 1440
GTGTGGGGGT GAGGTGGTTC CCCACAGGGG CAAAGCAGAG GCCACCCAAT GAGGATGGGC 1500
TGTGATCAGC AACTGGGCAA AACAGCCGAT GTCTATTACA GTTAGTTCTG GGCCAGAATG 1560
AGTAATGACT CGGTGATCAT GTTTGGTTTT CTAGGGAGCC AGCCTAGGGT GCCTGCCTCC 1620
AACTGGCTTT TCTAGGAGGG ATCCTCAGTG GAGAAGCCAT TCCCCACTGT CTAGATGGCC 1680
CAAGGCACAG AGCCAGGAGT GGCCTGGGGT TCACAGTGGC TGGTGCACAT ATCTCCTGCA 1740
CACTCACAGC CATGTTAATG TGTCCTGAAG GGAGAAGTCT ACCCTTGCAA TTTCCAGATA 1800
TTGGGACATG CTGTCCCTAC 1820
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